Canonical Allele Identifier: PA2827974451
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg625Met
CA16025598
NM_001354899.2:c.1874G>T